Cas 121682-63-1,[(2R,3R,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyloxy)-tetrahydro-pyran-3-yl]-carbamic acid benzyl ester

121682-63-1

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Basic information

Product Name: [(2R,3R,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyloxy)-tetrahydro-pyran-3-yl]-carbamic acid benzyl ester
Synonyms: [(2R,3R,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyloxy)-tetrahydro-pyran-3-yl]-carbamic acid benzyl ester
CAS NO:121682-63-1
Molecular Formula:
Molecular Weight: 721.934
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: [(2R,3R,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyloxy)-tetrahydro-pyran-3-yl]-carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(2R,3R,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyloxy)-tetrahydro-pyran-3-yl]-carbamic acid benzyl ester(121682-63-1)
EPA Substance Registry System: [(2R,3R,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyloxy)-tetrahydro-pyran-3-yl]-carbamic acid benzyl ester(121682-63-1)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 121682-63-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 121682-63-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,6,8 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 121682-63:
(8*1)+(7*2)+(6*1)+(5*6)+(4*8)+(3*2)+(2*6)+(1*3)=111
111 % 10 = 1
So 121682-63-1 is a valid CAS Registry Number.

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121682-63-1Relevant academic research and scientific papers

A Novel Glycosylation Reaction of 2-Amino-2-deoxy-D-glucopyranose Using Dimethylphosphinothioate

Inazu, Toshiyuki,Yamanoi, Takashi

, p. 69 - 72 (2007/10/02)

β-Glucosides were stereoselectively obtained in good yields from 3,4,6-tri-O-benzyl-2-benzyloxycarbonylamino-2-deoxy-α-D-glucopyranosyl dimethylphosphinothioate with several alcohols in the presence of iodine and a catalytic amount of trityl or perchlorat

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